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rs1064796267

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTT;CTT) 0 common in clinvar
Chromosome22
Position46350337
GeneTRMU
is asnp
is mentioned by
dbSNPrs1064796267
dbSNP (old)rs1064796267
ClinGenrs1064796267
ebirs1064796267
HLIrs1064796267
Exacrs1064796267
Gnomadrs1064796267
Varsomers1064796267
Maprs1064796267
PheGenIrs1064796267
Biobankrs1064796267
1000 genomesrs1064796267
hgdprs1064796267
ensemblrs1064796267
gopubmedrs1064796267
geneviewrs1064796267
scholarrs1064796267
googlers1064796267
pharmgkbrs1064796267
gwascentralrs1064796267
openSNPrs1064796267
23andMers1064796267
23andMe allrs1064796267
SNPshotrs1064796267
SNPdbers1064796267
MSV3drs1064796267
GWAS Ctlgrs1064796267
Max Magnitude0
ClinVar
Risk rs1064796267(-;-)
Alt rs1064796267(-;-)
Reference Rs1064796267(CTT;CTT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TRMU
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.46746234_46746236delCTT
CLNSRC
CLNACC RCV000482741.1,